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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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1-Octene → Chlorodimethyloctylsilane

HRID 989571
ノート
印刷プレビュー

反応式

HRID 989571 の反応式
[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH3:9][SiH:10]([CH3:12])[Cl:11]>[H+].[H+].Cl[Pt-2](Cl)(Cl)(Cl)(Cl)Cl.C1(C)C=CC=CC=1>[CH2:1]([Si:10]([CH3:12])([CH3:9])[Cl:11])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 81251-OcteneHCID 66108Chlorodimethylsilane

生成物 1

HCID 87482Chlorodimethyloctylsilane収率 88%

試薬・触媒・溶媒 2

HCID 61859Chloroplatinic acid触媒HCID 1140Toluene溶媒

反応条件

温度
70 °C

実験手順

123 g (1.1 mol) 1 -octene and 100 microliters of a 2% toluene solution of chloroplatinic acid were placed in a 500-mL four-neck flask equipped with a stirrer, thermometer, addition funnel, and condenser and were heated to 70° C. After the temperature had been raised, the heating mantle was removed and 94.5 g (1 mol) dimethylchlorosilane was added dropwise from the addition funnel. Heat generation was observed immediately, and the dropwise addition was carried out gradually so as to avoid having the temperature of the reaction solution exceed 80° C. After the completion of this addition, the reaction was continued for 30 minutes at 80° C. Gas chromatographic analysis of the resulting reaction solution gave 88% octyldimethylchlorosilane. The reaction solution was cooled to room temperature and 200 g toluene was introduced. The addition funnel was then replaced with a Teflon tube and ammonia was bubbled in until the pH of the reaction solution reached 10. The ammonium chloride product was removed by filtration, and the filtrate was then distillatively purified at 160° C./0.5 mmHg to obtain the following disilazane in a purity of 98 weight %.

後処理

  1. customequipped with a stirrer
  2. additionthermometer, addition funnel, and condenser
  3. temperatureAfter the temperature had been raised
  4. customthe heating mantle was removed
  5. temperatureHeat generation
  6. additionthe dropwise addition
  7. customexceed 80° C
  8. additionAfter the completion of this addition
  9. customGas chromatographic analysis of the resulting reaction solution

出典と根拠

ORDレコード
ord-d64aa44f6f2d45baacf37b5781b162f3
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06458420B1

反応ノート

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